(Q33592910)

28 July 2017

title

A new syndrome of autosomal recessive nephropathy, deafness, and hyperparathyroidism (English)

1 reference

28 July 2017

1 reference

1 reference

Edwards BD

1

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28 July 2017

Patton MA

series ordinal

2

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28 July 2017

Dilly SA

series ordinal

3

1 reference

28 July 2017

Eastwood JB

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 May 1989

1 reference

Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

26

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28 July 2017

issue

5

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28 July 2017

page(s)

289-293

1 reference

Urticaria, deafness, and amyloidosis: a new heredo-familial syndrome

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015593

Alport's syndrome. A report of 58 cases and a review of the literature

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015593

Prolactinoma: a question of rational treatment

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015593

Genetic heterogeneity of Alport syndrome.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015593

Familial nephrosis, nerve deafness, and hypoparathyroidism

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015593

Familial nephrosis associated with deafness and congenital urinary tract anomalies in siblings.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015593

Hereditary Nephritis: A Re-examination of its Clinical and Genetic Features

30 October 2018

1 reference

12 December 2020

NEONATAL FAMILIAL PRIMARY HYPERPARATHYROIDISM

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12 December 2020

The clinical spectrum of hereditary nephritis

1 reference

12 December 2020

Alport's syndrome or hereditary nephritis?

1 reference

12 December 2020

Autosomal recessive inheritance of familial hyperparathyroidism

1 reference

12 December 2020

Identifiers

PMC publication ID

1015593

1 reference

28 July 2017

1 reference